As Compliance Officer, you are reviewing GMP-documentation, and ensure compliance with GMP guidelines during the pharmaceutical production process. You have a broad role in documentation and compliance on the production floor.
Job description
You work in a large international QA-team and are responsible for the review of batch documentation and related GMP-documentation. You collaborate closely with the production team to ensure errors are corrected and prevented. To make sure the guidelines are followed closely, you do checks on the production floor. You take actions when GMP-procedures are not followed properly. Since you are working so closely with QA and production, you are highly involved with deviations, investigations, and CAPAs. Overall, you have a broad role in quality to ensure compliance, and are present in the office, and on the floor.
Responsibilities
- Ensure compliance of the production department
- Batch record reviews
- Inspections on the production floor
- Investigations
- CAPAs
- Collaborate with QA and with production
Profile
- Bachelor or University-level degree in Biotech or a pharmaceutical field
- GMP-working experience
- Knowledge of biopharmaceutical production is a huge plus, but not necessarily required
Benefits
- Long term position, direct hire by our client
- Salary range: €3500 - €5000, scaled based upon previous experience
- Daytime position, fulltime
- Occasional remote work possible after training period
- Location: Amsterdam
